EP0111863A1 - Process for the production of beta,4-dichloro-propiophenone - Google Patents
Process for the production of beta,4-dichloro-propiophenone Download PDFInfo
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- EP0111863A1 EP0111863A1 EP83112470A EP83112470A EP0111863A1 EP 0111863 A1 EP0111863 A1 EP 0111863A1 EP 83112470 A EP83112470 A EP 83112470A EP 83112470 A EP83112470 A EP 83112470A EP 0111863 A1 EP0111863 A1 EP 0111863A1
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- Prior art keywords
- reaction
- chloride
- lewis acid
- chlorobenzoyl chloride
- ethylene
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
Definitions
- the present invention relates to a new process for the preparation of ⁇ , 4-dichloropropiophenone.
- ⁇ , 4-dichloro-propiophenone can be prepared in good yield and high purity by reacting 4-chlorobenzoyl chloride with ethylene under pressure in a diluent in the presence of a Lewis acid if the reaction is not carried out in the presence of more than the stoichiometric amount of Lewis acid (based on 4-chlorobenzoyl chloride) in the temperature range from 30 to 100 ° C and at pressures from 0.1 to 100 bar.
- the method according to the invention has a number of advantages. So you get the ß, 4-dichloropropiophenone isomerically pure and can do without a complex separation and purification from the accompanying ß, 2-dichloropropiophenone. The reaction times are only a few hours and the yields are almost quantitative.
- the course of the reaction can be represented by the following formula:
- All inert organic solvents can be used as diluents. These preferably include halogenated hydrocarbons such as dichloromethane, chloroethane, 1,2-dichloroethane, 1,2-dichlorobenzene or trichlorobenzene; Nitroalkanes such as nitromethane, nitroethane or nitropropane; Nitrobenzene and carbon disulfide.
- Suitable catalysts are Lewis acids, such as those listed in Table 1, for example in Houben-Weyl, "Methods of Organic Chemistry", Volume VII / 2a, Georg Thieme Verlag Stuttgart 1973, on page 22/23.
- Aluminum chloride, iron chloride, zinc chloride, titanium tetrachloride and tin tetrachloride are preferred.
- Aluminum chloride is particularly preferably used as Lewis acid. The amount of Lewis acid used, which, based on 4-chlorobenzoyl chloride, is only used up to the equimolar amount.
- the reaction temperatures can be varied in the range from 30 to 100 ° C., preferably 30 to 70 ° C.
- Ethylene is introduced or pressed under pressure, the pressure being varied between 0.1 and 100 bar, preferably 1 to 20 bar.
- the reactants 4-chlorobenzoyl chloride and ethylene are reacted in a molar ratio of 0.5: 1 to 2: 1, preferably 1: 1.
- the phases are separated, the organic phase is washed with dilute hydrochloric acid, then with soda solution at 25 to 30 ° C., furthermore with 150 ml of water.
- the organic phase (599 g) is distilled to an approximately 50% solution and added to determine the content, yield 96.6%.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
Die vorliegende Erfindung betrifft ein neues Verfahren zur Herstellung von ß,4-Dichlor-propiophenon.The present invention relates to a new process for the preparation of β, 4-dichloropropiophenone.
Es ist bereits bekannt, ß,4-Dichlor-propiophenon durch eine Friedel-Crafts-Acylierung von Chlorbenzol und 3-Chlorpropionsäurechlorid herzustellen (J. Org. Chem. 12, 96 (1947); Canad. J. Res. 8, 440 (1933)). Dieses Verfahren hat jedoch den Nachteil, daß neben dem erwünschten 4-Chlor-Derivat auch das isomere 2-Chlor-Derivat entsteht, welches nur schwierig und unter großem Aufwand vom ß,4-Dichlor-propiophenon abgetrennt werden kann.It is already known to produce β, 4-dichloropropiophenone by Friedel-Crafts acylation of chlorobenzene and 3-chloropropionic acid chloride (J. Org. Chem. 12, 96 (1947); Canad. J. Res. 8, 440 ( 1933)). However, this process has the disadvantage that, in addition to the desired 4-chloro derivative, the isomeric 2-chloro derivative also arises, which can be separated from the β, 4-dichloro-propiophenone only with difficulty and with great effort.
Es ist ferner bekannt, ß-Chlor-propiophenon durch Addition von Ethylen an Benzoylchlorid in Gegenwart von Aluminiumchlorid in Ethylbromid herzustellen (Canad. J. Res. 8, 440 (1933)). In der selben Publikation werden 10 substituierte ß-Chlorpropiophenone, u.a. auch ß,4-Dichlor-propiophenon, beschrieben, die jedoch überraschenderweise nicht durch Addition von Ethylen an substituierte Benzoylchloride, sondern durch Friedel-Crafts-Acylierung von substituierten Benzolen und 3-Chlorpropionsäurechlorid hergestellt werden (Canad. J. Res. 8, 440 (1933)). Die Übertragung der für Benzoylchlorid gemachten Vorschrift auf 4-Chlorbenzoylchlorid zur Herstellung von ß,4-Dichlor-propiophenon ergab ein durch Oligomerisierung von Ethylen verunreinigtes Produkt, das sich nicht ausreichend reinigen ließ. Ein weiterer Nachteil des oben beschriebenen Verfahrens besteht in den erforderlichen Reaktionszeiten von 30 bis 35 Stunden für einen 0,4 Mol-Ansatz bei 20°C.It is also known to produce β-chloropropiophenone by adding ethylene to benzoyl chloride in the presence of aluminum chloride in ethyl bromide (Canad. J. Res. 8, 440 (1933)). In the same publication 10 substituted ß-chloropropiophenones, ß, 4-dichloropropiophenone, among others, has been described, which, however, is surprisingly not produced by adding ethylene to substituted benzoyl chlorides, but rather by Friedel-Crafts acylation of substituted benzenes and 3-chloropropionic acid chloride (Canad. J. Res. 8, 440 (1933)). The transfer of the instructions made for benzoyl chloride to 4-chlorobenzoyl chloride for the production of β, 4-dichloropropiophenone resulted in a product contaminated by oligomerization of ethylene which could not be adequately cleaned. Another disadvantage of the process described above is the required reaction times of 30 to 35 hours for a 0.4 mol batch at 20 ° C.
Es wurde jetzt gefunden, daß man ß,4-Dichlor-propiophenon in guter Ausbeute und hoher Reinheit durch Umsetzung von 4-Chlorbenzoylchlorid mit Ethylen unter Druck in einem Verdünnungsmittel in Gegenwart einer Lewis-Säure herstellen kann, wenn man die Umsetzung in Gegenwart von nicht mehr als der stöchiometrischen Menge Lewis-Säure (bezogen auf 4-Chlorbenzoylchlorid) im Temperaturbereich von 30 bis 100°C und bei Drücken von 0,1 bis 100 bar durchführt.It has now been found that β, 4-dichloro-propiophenone can be prepared in good yield and high purity by reacting 4-chlorobenzoyl chloride with ethylene under pressure in a diluent in the presence of a Lewis acid if the reaction is not carried out in the presence of more than the stoichiometric amount of Lewis acid (based on 4-chlorobenzoyl chloride) in the temperature range from 30 to 100 ° C and at pressures from 0.1 to 100 bar.
Es ist als ausgesprochen überraschend zu bezeichnen, daß das Verfahren zur Herstellung von ß-Chlorpropiophenon aus Benzoylchlorid und Ethylen (Canad. J. Res. 8, 440 (1933)) sich nicht zur analogen Herstellung von ß,4-Dichlor-propiophenon eignet. Wird statt des Überschusses an Aluminiumchlorid als Katalysator nur die äquimolare Menge an Lewis-Säure (bezogen auf 4-Chlorbenzoylchlorid) verwendet, so verläuft die Addition von Ethylen an 4-Chlorbenzoylchlorid selektiv zum ß,4-Dichlor-propiophenon. Es war ebenfalls nicht zu erwarten, daß die Steigerung der Temperatur auf Werte über 30°C die Selektivität für die Ketonbildung, obgleich die thermische Unbeständigkeit dieser ß-Chlorketone bekannt ist, erhöht. ("The ß-chloroketone is easily decomposed by heat." Canad. J. Res. 8, 440, Zeile 21 (1933)).It can be described as extremely surprising that the process for the preparation of β-chloropropiophenone from benzoyl chloride and ethylene (Canad. J. Res. 8, 440 (1933)) is not suitable for the analogous preparation of β, 4-dichloropropiophenone. Instead of the excess of aluminum chloride as the catalyst, only the equimolar amount of Lewis acid (based on 4-chlorobenzoyl chloride) is used, the addition of ethylene to 4-chlorobenzoyl chloride is selective to the ß, 4-dichloropropiophenone. It was also unlikely that increasing the temperature above 30 ° C would increase the selectivity for ketone formation, although the thermal instability of these β-chloro ketones is known. ("The β-chloroketone is easily decomposed by heat." Canad. J. Res. 8, 440, line 21 (1933)).
Das erfindungsgemäße Verfahren weist eine Reihe von Vorteilen auf. So erhält man das ß,4-Dichlor-propiophenon isomerenrein und kann auf eine aufwendige Trennung und Reinigung vom begleitenden ß,2-Dichlor- propiophenon verzichten. Die Reaktionszeiten betragen nur wenige Stunden und die Ausbeuten sind nahezu quantitativ.The method according to the invention has a number of advantages. So you get the ß, 4-dichloropropiophenone isomerically pure and can do without a complex separation and purification from the accompanying ß, 2-dichloropropiophenone. The reaction times are only a few hours and the yields are almost quantitative.
Der Reaktionsablauf kann durch das folgende Formelschema wiedergegeben werden:
Als Katalysatoren kommen Lewis-Säuren in Frage, wie sie beispielsweise in Houben-Weyl, "Methoden der organischen Chemie", Band VII/2a, Georg Thieme Verlag Stuttgart 1973, auf Seite 22/23 in Tabelle 1 aufgeführt sind. Bevorzugt seien Aluminiumchlorid, Eisenchlorid, Zinkchlorid, Titantetrachlorid und Zinntetrachlorid genannt. Besonders bevorzugt wird Aluminiumchlorid als Lewis-Säure eingesetzt. Bedeutungsvoll ist die eingesetzte Menge an Lewis-Säure, die bezogen auf 4-Chlorbenzoylchlorid nur bis zur äquimolaren Menge verwendet wird.Suitable catalysts are Lewis acids, such as those listed in Table 1, for example in Houben-Weyl, "Methods of Organic Chemistry", Volume VII / 2a, Georg Thieme Verlag Stuttgart 1973, on page 22/23. Aluminum chloride, iron chloride, zinc chloride, titanium tetrachloride and tin tetrachloride are preferred. Aluminum chloride is particularly preferably used as Lewis acid. The amount of Lewis acid used, which, based on 4-chlorobenzoyl chloride, is only used up to the equimolar amount.
Die Reaktionstemperaturen können im Bereich von 30 bis 100°C, vorzugsweise 30 bis 70°C, variiert werden.The reaction temperatures can be varied in the range from 30 to 100 ° C., preferably 30 to 70 ° C.
Ethylen wird unter Druck eingeleitet oder aufgepreßt, wobei der Druck zwischen 0,1 und 100 bar, vorzugsweise 1 bis 20 bar, variiert wird.Ethylene is introduced or pressed under pressure, the pressure being varied between 0.1 and 100 bar, preferably 1 to 20 bar.
Bei der Durchführung des erfindungsgemäßen Verfahrens setzt man die Reaktionspartner 4-Chlorbenzoylchlorid und Ethylen in einem Molverhältnis von 0,5 : 1 bis 2 : 1, vorzugsweise 1 : 1, um.When carrying out the process according to the invention, the reactants 4-chlorobenzoyl chloride and ethylene are reacted in a molar ratio of 0.5: 1 to 2: 1, preferably 1: 1.
ß,4-Dichlor-propiophenon dient als Ausgangsstoff zur Herstellung von optischen Aufhellern (DE-A 2 310 446).β, 4-dichloropropiophenone is used as the starting material for the production of optical brighteners (DE-A 2 310 446).
26,7 g (0,2 mol) gepulvertes Aluminiumchlorid werden in 100 rnl destilliertem Methylenchlorid im Autoklaven (V4A) bei 25°C unter N2 vorgelegt. Nach Zugabe von 35,0 g (0,2 mol) p-Chlorbenzoylchlorid wird auf 50°C erwärmt und 10 bar Ethylen aufgedrückt. Nach 3 Stunden ist Druckkonstanz erreicht. Die Reaktionslösung wird mit CH2C12 verdünnt und mit Eis sowie verdünnter Salzsäure aufgearbeitet. Nach dem Trocknen der Lösung über Natriumsulfat wird das Lösungsmittel im Vakuum abgezogen. Es bleiben 36,8 g (0,18 mol, 90%) ß,4-Dichlor-propiophenon als Ö1 zurück, das langsam durchkristallisiert (GC-Reinheit 98%). Fp. 47 bis 49°C (Beilstein VII/3, S. 1030: Fp. 48°C).26.7 g (0.2 mol) of powdered aluminum chloride are placed in 100 ml of distilled methylene chloride in an autoclave (V4A) at 25 ° C. under N2. After adding 35.0 g (0.2 mol) of p-chlorobenzoyl chloride, the mixture is heated to 50 ° C. and 10 bar of ethylene are injected. Pressure is constant after 3 hours. The reaction solution is diluted with CH 2 C1 2 and worked up with ice and dilute hydrochloric acid. After drying the solution over sodium sulfate, the solvent is removed in vacuo. 36.8 g (0.18 mol, 90%) of β, 4-dichloro-propiophenone remain as Ö1, which slowly crystallizes through (GC purity 98%). Mp 47 to 49 ° C (Beilstein VII / 3, p. 1030: mp 48 ° C).
NMR (CDC1,); d 3,4 (t, J = 6,5 Hz, 2 H), 3,9 (t, J 6,5 Hz, 2 H), 7,4 (d, J = 9 Hz, 2 H), 7,9 (d, J = 9 Hz, 2 H)NMR (CDC1,); d 3.4 (t, J = 6.5 Hz, 2 H), 3.9 (t, J 6.5 Hz, 2 H), 7.4 (d, J = 9 Hz, 2 H), 7 , 9 (d, J = 9 Hz, 2 H)
176,5 g ( 1 Mol) 99,1 %iges 4-Chlorbenzoylchlorid werden zu einer Suspension von 134 g (0,975 Mol) 97 %igem Aluminiumchlorid wasserfrei in 180 g o-Dichlorbenzol (wasserfrei, andestilliert) unter Rühren und Feuchtigkeitsausschluß getropft, wobei sich das Gemisch auf 44°C erwärmt. Durch Umsetzen dieses Gemisches mit gasförmigem Ethylen unter Rühren bei 50°C unter einem Druck von 2 bar in einem Email-Autoklaven erhält man nach 6 Stunden und 45 Minuten ein Reaktionsgemisch, das beim Austragen in eine wäßrige Salzsäure (aus 600 rnl Wasser und 100 ml konzentrierter Salzsäure) bei 50°C hydrolysiert wird. Man trennt die Phasen, wäscht die organische Phase mit verdünnter Salzsäure, danach mit Soda-Lösung bei 25 bis 30°C, ferner mit 150 rnl Wasser. Die organische Phase (599 g) wird bis zu einer ca. 50 %igen Lösung andestilliert und zur Gehaltsbestimmung gegeben, Ausbeute 96,6 %.176.5 g (1 mol) of 99.1% 4-chlorobenzoyl chloride are added dropwise to a suspension of 134 g (0.975 mol) of 97% aluminum chloride in 180 g of o-dichlorobenzene (anhydrous, distilled) while stirring and excluding moisture, with the mixture warms to 44 ° C. By reacting this mixture with gaseous ethylene with stirring at 50 ° C. under a pressure of 2 bar in an enamel autoclave, a reaction mixture is obtained after 6 hours and 45 minutes, which mixture is discharged into an aqueous hydrochloric acid (from 600 ml Water and 100 ml of concentrated hydrochloric acid) is hydrolyzed at 50 ° C. The phases are separated, the organic phase is washed with dilute hydrochloric acid, then with soda solution at 25 to 30 ° C., furthermore with 150 ml of water. The organic phase (599 g) is distilled to an approximately 50% solution and added to determine the content, yield 96.6%.
68,6 g( 0,5 Mol) 97 %iges Aluminiumchlorid (gepulvert) werden in 200 rnl wasserfreiem o-Dichlorbenzol bei 25°C suspendiert. Zu dieser Mischung tropft man innerhalb 30 Minuten 89,5 g (0,5 Mol) 98 %iges 4-Chlorbenzoylchlorid unter Rühren und schwachem Kühlen. Die so hergestellte Lösung des Aluminiumchlorid-Komplexes wird in einem Einliter-Glasautoklaven unter Rühren auf 50°C erwärmt und durch Aufdrücken von gasförmigem Ethylen bis zu einem Druck von maximal 6 bar innerhalb 2 1/4 Stunden umgesetzt. Man rührt das Gemisch nach 1,5 Stunden nach, entspannt den Druckbehälter und trägt den Inhalt auf ca. 600 g Eis aus, wobei man 10 rnl konzentrierte Salzsäure zugibt. Man trennt die Phasen, wäscht die organische Phase zweimal mit je 50 ml Wasser, vereint die wäßrigen Phasen und schüttelt sie zweimal mit jeweils 50 rnl o-Dichlorbenzol aus. Die vereinigten organischen Lösungen werden über eine einfache Destillationsbrücke im Wasserstrahlvakuum destilliert, bis eine etwa 50 %ige Lösung von ß,4-Dichlor-propiophenon als Sumpf vorliegt. Ausbeute: 199,6 g Lösung mit einem Gehalt von 619 g/l ≙ 94 % d.Th.68.6 g (0.5 mol) of 97% aluminum chloride (powdered) are suspended in 200 ml of anhydrous o-dichlorobenzene at 25 ° C. 89.5 g (0.5 mol) of 98% 4-chlorobenzoyl chloride are added dropwise to this mixture over the course of 30 minutes, with stirring and gentle cooling. The solution of the aluminum chloride complex thus prepared is heated in a one-liter glass autoclave with stirring to 50 ° C. and reacted by pressing in gaseous ethylene up to a pressure of 6 bar within 2 1/4 hours. The mixture is stirred after 1.5 hours, the pressure vessel is released and the contents are poured onto about 600 g of ice, 10 ml of concentrated hydrochloric acid being added. The phases are separated, the organic phase is washed twice with 50 ml of water each time, the aqueous phases are combined and shaken out twice with 50 ml of o-dichlorobenzene in each case. The combined organic solutions are distilled over a simple distillation bridge in a water jet vacuum until an approximately 50% solution of β, 4-dichloropropiophenone is present as the bottom. Yield: 199.6 g solution with a content of 619 g / l ≙ 94% of theory
Claims (6)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19823247823 DE3247823A1 (en) | 1982-12-23 | 1982-12-23 | METHOD FOR PRODUCING SS, 4-DICHLOR-PROPIOPHENONE |
DE3247823 | 1982-12-23 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0111863A1 true EP0111863A1 (en) | 1984-06-27 |
EP0111863B1 EP0111863B1 (en) | 1985-08-07 |
Family
ID=6181630
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP83112470A Expired EP0111863B1 (en) | 1982-12-23 | 1983-12-12 | Process for the production of beta,4-dichloro-propiophenone |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0111863B1 (en) |
JP (1) | JPS59118729A (en) |
DE (2) | DE3247823A1 (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE733694C (en) * | 1935-11-13 | 1943-04-01 | Ig Farbenindustrie Ag | Process for the production of halogenated ketones |
DE1768624A1 (en) * | 1967-06-09 | 1971-11-18 | Shell Int Research | Process for the preparation of halophenylacetophenones |
DE2851371B1 (en) * | 1978-11-28 | 1980-05-29 | Hoechst Ag | Process for the production of ketones |
-
1982
- 1982-12-23 DE DE19823247823 patent/DE3247823A1/en not_active Withdrawn
-
1983
- 1983-12-12 EP EP83112470A patent/EP0111863B1/en not_active Expired
- 1983-12-12 DE DE8383112470T patent/DE3360527D1/en not_active Expired
- 1983-12-19 JP JP58238074A patent/JPS59118729A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE733694C (en) * | 1935-11-13 | 1943-04-01 | Ig Farbenindustrie Ag | Process for the production of halogenated ketones |
DE1768624A1 (en) * | 1967-06-09 | 1971-11-18 | Shell Int Research | Process for the preparation of halophenylacetophenones |
DE2851371B1 (en) * | 1978-11-28 | 1980-05-29 | Hoechst Ag | Process for the production of ketones |
Non-Patent Citations (1)
Title |
---|
CANADIAN JOURNAL OF RESEARCH, vol.VIII, 1933, published by the NATIONAL RESEARCH COUNCIL OF CANADA C.F.H. ALLEN et al. "The preparation of b-chloropropiopheNONE" SEITEN 440-446 *SEITEN 440,443, 444* * |
Also Published As
Publication number | Publication date |
---|---|
DE3247823A1 (en) | 1984-06-28 |
JPH0153857B2 (en) | 1989-11-15 |
JPS59118729A (en) | 1984-07-09 |
EP0111863B1 (en) | 1985-08-07 |
DE3360527D1 (en) | 1985-09-12 |
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